Mannheim, 68167, Germany
NCT Number: NCT02274376
Non-Interventional Study of Xeloda (Capecitabine) in Patients With Gastric Cancer
This observational study will collect prospective data on the safety and tolerability of Xeloda in patients with advanced gastric cancer from every day clinical practice. Documentation of treatment for each patient is to continue until the end of treatment per oncologist's assessment.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patients aged >/=18 years, with metastatic gastric cancer who are available for prospective documentation of their treatment (first-line chemotherapy)
- Informed consent
Exclusion criteria
- Contraindications to Xeloda per the Summary of Product Characteristics (SmPC)
Treatment and study plan
Primary outcomes
-
Progression-free survival
Time frame: Up to 4 years
-
Safety and tolerability: incidence and nature of adverse drug reactions
Time frame: Up to 4 years
Secondary outcomes
-
Proportion of patients with modifications in Xeloda dosing
Time frame: Up to 4 years
-
Average duration of treatment
Time frame: Up to 4 years
-
Number of modifications in chosen regimen combination therapy
Time frame: Up to 4 years
-
Incidence and nature of dose interruptions
Time frame: Up to 4 years
Sponsors and collaborators
Lead sponsor
Hoffmann-La Roche
Industry
Registry information
Official study title
NIS Xeloda in Gastric Cancer
Important dates
- Study start
- 2008
- Primary completion
- 2012
- Study completion
- 2012
- First posted
- Oct 24, 2014
- Registry last updated
- Nov 2, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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